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Lamprien Provence

FDA import alert and refusal historySenas, FranceFEI 3004350711

Recorded by FDA as LAMPRIEN PROVENCE

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Example subjectLamprien Provenc added to Import Alert 16-129 (red list)

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As of October 25, 2026, Lamprien Provence (Senas, France) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for mix spice & seasoning (barbeque mix); herbs de provence, published by FDA on September 16, 2009, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Lamprien Provence

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 99-19red listmix spice & seasoning (barbeque mix); Herbs de Provence
    Source

Questions about Lamprien Provence

Is Lamprien Provence on an FDA import alert?
Yes. As of October 25, 2026, Lamprien Provence is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for mix spice & seasoning (barbeque mix); herbs de provence; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Lamprien Provence?
No FDA import refusals for Lamprien Provence appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Lamprien Provence's FEI number?
Lamprien Provence's FDA Establishment Identifier (FEI) is 3004350711.
Can shipments from Lamprien Provence still enter the U.S.?
Shipments of mix spice & seasoning (barbeque mix); herbs de provence from Lamprien Provence can be detained without physical examination under Import Alert 99-19; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectLamprien Provenc added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.